A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055263



Internal ID19144482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40854453..40891756hg38UCSC Ensembl
Innerchr19:41360358..41397661hg19UCSC Ensembl
Innerchr19:46052198..46089501hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3837304
hg1937304
hg1837304
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3539n100
Supporting Variantsnssv3567392
Samples
Known GenesCYP2A7, CYP2G1P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055263
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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